A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145676



Internal ID21473242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97971638..97971693hg38UCSC Ensembl
chr7:97600950..97601005hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568109
Supporting Variants
SamplesHG03371
Known GenesMGC72080
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145676
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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